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Filtres: Author is Benammar, Nawal [Enlever les filtres]

2008

Six I, Hermida J-S, Huang H, Gouas L, Fressart V, Benammar N, Hainque B, Denjoy I, Chahine M, Guicheney P. The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases. Europace. 2008;10(1):79-85.

2003

Keller DI, Acharfi S, Delacrétaz E, Benammar N, Rotter M, Pfammatter JPi, Fressart V, Guicheney P, Chahine M. A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation. J Mol Cell Cardiol. 2003;35(12):1513-21.

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